دورية أكاديمية

Two predominant molecular subtypes of spinal meningioma: thoracic NF2‑mutant tumors strongly associated with female sex, and cervical AKT1‑mutant tumors originating ventral to the spinal cord

التفاصيل البيبلوغرافية
العنوان: Two predominant molecular subtypes of spinal meningioma: thoracic NF2‑mutant tumors strongly associated with female sex, and cervical AKT1‑mutant tumors originating ventral to the spinal cord
المؤلفون: Hua, Lingyang, Alkhatib, Majd, Podlesek, Dino, Günther, Leila, Pinzer, Thomas, Meinhardt, Matthias, Zeugner, Silke, Herold, Sylvia, Cahill, Daniel P., Brastianos, Priscilla K., Williams, Erik A., Clark, Victoria E., Shankar, Ganesh M., Wakimoto, Hiroaki, Ren, Leihao, Chen, Jiawei, Gong, Ye, Schackert, Gabriele, Juratli, Tareq A.
حالة النشر: publishedVersion
بيانات النشر: Springer, 2022.
سنة النشر: 2022
المجموعة: Hochschulschriftenserver (HSSS) der SLUB Dresden
Original Material: urn:nbn:de:bsz:14-qucosa2-910475
مصطلحات موضوعية: thoracic NF2‑mutant tumors, cervical AKT1‑mutant tumors, Spinal meningiomas (SM), primary meningiomas, spinal intradural tumors, thorakale NF2-mutierte Tumoren, zervikale AKT1-mutierte Tumoren, spinale Meningeome (SM), primäre Meningeome, spinale intradurale Tumore, info:eu-repo/classification/ddc/610, ddc:610
الوصف: Spinal meningiomas (SM) comprise 5–10% of primary meningiomas and up to 30% of spinal intradural tumors. SMs are usually sporadic, but rarely, they can develop in association with genetic diseases like neurofibromatosis type 2 or schwannomatosis [2, 4, 6]. While the mutational landscape of intracranial meningiomas has been extensively studied [3, 5, 11, 14], our understanding of the molecular profile of SM remains incomplete. To date, genomic studies in SMs have been underpowered to make significant conclusions about the correlations between main genomic driver alterations and clinical features of these tumors. Here, we sought to assess the mutational profile of WHO grade 1 SM and to investigate the clinical characteristics that correlate with the genomic status.
Original Identifier: oai:qucosa:de:qucosa:91047
نوع الوثيقة: Article
اللغة: English
تدمد: 1432-0533
DOI: 10.1007/s00401-022-02474-9
الإتاحة: https://tud.qucosa.de/id/qucosa%3A91047Test
https://tud.qucosa.de/api/qucosa%3A91047/attachment/ATT-0Test/
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsndl.DRESDEN.oai.qucosa.de.qucosa.91047
قاعدة البيانات: Networked Digital Library of Theses & Dissertations
الوصف
تدمد:14320533
DOI:10.1007/s00401-022-02474-9